Penumbra, Inc.
Web: http://www.penumbrainc.com
E-Mail:
Address: 1351 Harbor Bay Parkway, Alameda, California 94502, USA
Phone: +1-(510)-618-3223 | Fax: +1-(510)-748-3232 | Map/Directions >>
Profile: Penumbra, Inc. is a medical device company. We develop and manufacture minimally invasive medical devices for cerebrovascular diseased patients. Our products are Penumbra System™ and Neuron System™. The Neuron intracranial access system allows higher placement in the neuro anatomy to provide robust anatomical support through enhanced catheter to vessel wall engagement. We offer Neuron 6F 070-lumen delivery catheter, 5F select catheter, and 6f 053-lumen delivery catheter. The Neuron 5F select catheter has stainless steel braided proximal shafts for support and torque response, with a soft polymer distal shaft to enable atraumatic vessel selection. The Penumbra system uses a unique micro catheter and Separator™ based thrombus-debulking approach to intracranial vessel revascularization.
FDA Registration Number: 3005168196
7 Products/Services (Click for related suppliers)
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| • AC-Powered Portable Ward Use Suction Apparatus (FDA Code: JCX / 878.4780) A powered suction pump is a portable, AC-powered or compressed air-powered device intended to be used to remove infectious materials from wounds or fluids from a patient's airway or respiratory support system. The device may be used during surgery in the operating room or at the patient's bedside. The device may include a microbial filter. |
| • General Medical Device |
| • Intracranial Access Systems |
| • Manual/Powered Portable Aspiration Pump (FDA Code: BTA / 878.4780) |
| • Medical Devices |
| • Percutaneous Catheter (FDA Code: DQY / 870.1250) A percutaneous catheter is a device that is introduced into a vein or artery through the skin using a dilator and a sheath (introducer) or guide wire. |
| • Thrombus Retriever Catheter (FDA Code: NRY / 870.1250) |
